A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844632



Internal ID22619567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142648595..142653393hg38UCSC Ensembl
chr6:142969732..142974530hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg384799
hg194799
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501827
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844632
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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